Basic information Safety Supplier Related

N-Carbethoxy-4-tropinone

Basic information Safety Supplier Related

N-Carbethoxy-4-tropinone Basic information

Product Name:
N-Carbethoxy-4-tropinone
Synonyms:
  • n-(carboethoxy)tropinone
  • 3-Oxo-8-azabicylo[3.2.1]octane-8-carboxylic acid
  • ethyl 3-oxo-8-azabicyclo(3.2.1)octane-8-carboxylate
  • N-(Carboethoxy)tropinone~3-Oxo-8-azabicyclo[3.2.1]octane-8-carboxylic acid ethyl ester
  • N-ethoxycarbonylnortropan-3-one
  • N-(Ethoxycarbonyl)tropinone,99%
  • N-(ETHOXYCAZBONYL)NORTROPINONE
  • N-(Ethoxycarbonyl)nortropinone, 99%
CAS:
32499-64-2
MF:
C10H15NO3
MW:
197.23
EINECS:
1312995-182-4
Product Categories:
  • Miscellaneous Biochemicals
Mol File:
32499-64-2.mol
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N-Carbethoxy-4-tropinone Chemical Properties

Boiling point:
152-153°C 11mm
Density 
1.1575 (rough estimate)
refractive index 
1.4876-1.4896
Flash point:
152-153°C/11mm
storage temp. 
Sealed in dry,Room Temperature
pka
-1.66±0.20(Predicted)
form 
Liquid
color 
Clear slightly yellow to light brown
BRN 
1530944
CAS DataBase Reference
32499-64-2(CAS DataBase Reference)
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Safety Information

Safety Statements 
24/25
HS Code 
29399990

MSDS

  • Language:English Provider:ACROS
  • Language:English Provider:ALFA
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N-Carbethoxy-4-tropinone Usage And Synthesis

Chemical Properties

CLEAR SLIGHTLY YELLOW TO LIGHT BROWN LIQUID

Synthesis

532-24-1

541-41-3

32499-64-2

To a dry 500 mL round-bottomed flask were added a stirrer, 8-methyl-8-azabicyclo[3.2.1]octan-3-one (10.0 g, 0.072 mol) and potassium carbonate (0.050 g). Anhydrous toluene (90 mL) was added, followed by slow dropwise addition of ethyl chloroformate (21 mL, 0.22 mol) via syringe. A condenser tube and nitrogen bubbler were installed and the reaction was heated to reflux with stirring overnight. Upon completion of the reaction, the mixture was concentrated under reduced pressure and the resulting brown oil was dissolved in dichloromethane (100 mL) and washed with water (100 mL). The organic and aqueous layers were separated in a partition funnel and the aqueous layer was extracted with dichloromethane (3 x 50 mL). The organic phases were combined, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane, 1:3) to afford ethyl 3-oxo-8-azabicyclo[3.2.1]octane-8-carboxylate (13.1 g, 92% yield) as a light yellow oil.1H NMR (δ): 4.51 (br s, 2H), 4.16 (q, J = 7.2 Hz, 2H), 2.63 (br s , 2H), 2.31 (dd, J = 17.4, 1.6 Hz, 2H), 2.07-2.03 (m, 2H), 1.65 (d, J = 7.6 Hz, 2H), 1.25 (t, J = 7.2 Hz, 3H).13C NMR (δ): 208.3, 154.1, 61.6, 53.2, 49.1, 29.5 (2), 28.8 (2), 14.8 (2), 28.8 (2), 29.5 (2), 29.5 (2), 28.8 (2), 28.8 (2), 28.8 (2), 29.5 (2) 28.8 (2), 14.9.

References

[1] Bioorganic and Medicinal Chemistry Letters, 2003, vol. 13, # 4, p. 629 - 632
[2] Journal of Heterocyclic Chemistry, 2004, vol. 41, # 4, p. 569 - 574
[3] Bioorganic and Medicinal Chemistry, 2011, vol. 19, # 24, p. 7551 - 7558
[4] Patent: CN105294674, 2016, A. Location in patent: Paragraph 0147; 0148; 0149
[5] Patent: WO2018/140876, 2018, A1. Location in patent: Page/Page column 216

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